Department of Otorhinolaryngology.
Department of Pathology, Tianjin Medical University General Hospital, Tianjin, PR China.
Medicine (Baltimore). 2021 May 7;100(18):e25782. doi: 10.1097/MD.0000000000025782.
Spindle cell lipoma is a rare, uncommon type of benign lipomatous tumor, a distinct group of lipomas composed of mature adipocytes, uniform spindle cells, and multinucleated giant cells associated with ropey collagen. Immunohistochemically, spindle cell lipoma is characterized by the diffuse expression of CD34.
We present a rare case of a 56-year-old man who complained of vomiting out of a smooth and giant mass in the oral cavity provoked by an intra-abdominal pressure increase. Oral examination revealed an elongated mass protruding from the mouth. Computed tomography of the patient showed a mass from left pyriform to oral cavity, with 2.38 × 2.78 × 16.86 cm in size. The flexible fiberscope showed that the pedicle of the elongated mass originated from the posterior wall of the hypopharynx, corresponding to the left pyriform fossa.
Histopathologically, the tumor was mainly composed of hyperplastic adipocytes, admixed with small blood vessels, and scattered inside adipose tissue spindle cells. The immunohistochemical profile revealed positivity of spindle cells for CD34, negativity for S100, and low proliferation with Ki67, which confirmed the diagnosis of spindle cell lipoma and revealed its benign behavior.
The patient underwent hypopharyngeal mass resection using transoral suspension laryngoscopy.
No recurrence was found after 5 months of follow-up.
Spindle cell lipoma is difficult to diagnose early because of slow growth and subtle symptomatology. This entity should be differentiated from several benign or malignant subtypes of lipomas, including liposarcomas. In this case, the spindle cell lipoma is large and originates from the hypopharynx, which is a rare entity and presents with atypical symptoms. This case gave rise to further studies on the clinical and pathologic characteristics of this tumor in the future.
梭形细胞脂肪瘤是一种罕见的、不常见的良性脂肪瘤,是一组由成熟脂肪细胞、均匀梭形细胞和与绳状胶原相关的多核巨细胞组成的独特脂肪肿瘤。免疫组化染色梭形细胞脂肪瘤的特征是弥漫性表达 CD34。
我们报告了 1 例罕见的 56 岁男性病例,他主诉因腹内压增加而呕吐出口腔内的光滑巨大肿块。口腔检查显示口腔内有一突出的长形肿块。患者的计算机断层扫描显示肿块从左梨状窝延伸至口腔,大小为 2.38×2.78×16.86cm。软性纤维喉镜检查显示,长形肿块的蒂部起源于下咽后壁,对应左梨状窝。
组织病理学上,肿瘤主要由增生的脂肪细胞组成,混杂有小血管,散布在脂肪组织内的梭形细胞。免疫组化显示梭形细胞 CD34 阳性,S100 阴性,Ki67 增殖率低,这证实了梭形细胞脂肪瘤的诊断,并显示其良性行为。
患者采用经口悬雍垂喉镜行下咽肿块切除术。
随访 5 个月未见复发。
梭形细胞脂肪瘤由于生长缓慢和症状微妙,早期诊断困难。该实体应与包括脂肪肉瘤在内的几种良性或恶性脂肪肿瘤亚型相区别。在本例中,梭形细胞脂肪瘤体积较大,起源于下咽,这是一种罕见的实体,表现出非典型的症状。该病例促使我们进一步研究该肿瘤的临床和病理特征。